PSORIAFORCE

Product NDC

43857-0338

11-digit product format

438570338

Labeler code

43857

Product ID

43857-0338_da5554bc-a0c4-458a-9dea-d97da0943111

Type

HUMAN OTC DRUG

Nonproprietary name

NOT APPLICABLE

Dosage form

LIQUID

Route

ORAL

Labeler

BioActive Nutritional, Inc.

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2014-10-15

Marketing end

0000-00-00

Substance

BAPTISIA TINCTORIA ROOT; BERBERIS VULGARIS ROOT BARK; ECHINACEA ANGUSTIFOLIA; GLYCYRRHIZA GLABRA; GOLDENSEAL; ARCTIUM LAPPA ROOT; PHYTOLACCA AMERICANA ROOT; FRANGULA ALNUS BARK; FRANGULA PURSHIANA BARK; TRIFOLIUM PRATENSE FLOWER; ZANTHOXYLUM AMERICANUM BARK; ARSENIC TRIIODIDE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; CLEMATIS RECTA FLOWERING TOP; GRAPHITE; POTASSIUM CHLORIDE; POTASSIUM SULFATE; DAPHNE MEZEREUM BARK; KEROSENE; SEPIA OFFICINALIS JUICE

Active strength

3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record